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A History of Neuropsychology


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target="_blank" rel="nofollow" href="#ulink_0bdc3daa-46a8-58d8-87b2-bc619c6167af">7, 8]. The author’s experience coincides with the opinion [9].

      Historical Background

      The existence of Gogi aphasia has been repeatedly confirmed in Japan [8]. Unfortunately, this has not been the case in Europe and America. This may be due to the difference of the mode of spoken language. Indo-European languages belong to a group called reflected language, while Japanese is one of the agglutinated languages in which semanteme (substantive words) and morpheme (grammatical words) are clearly separated [4].

      Neuropsychological Interpretation

      As for the fourth feature of Gogi aphasia, Imura’s stance was rather vague. Although he included it as one of the core features of Gogi aphasia, he was prudent to regard the difficulty as an integral part of the syndrome. Thus, in the original paper [1], he admitted that no complete correspondence between symptoms of speech and written language could be confirmed, since every case he had encountered did not necessarily show this pattern of difficulty in written language. But in the subsequent papers, he seemed to have gained confidence to claim that this particular pattern of kanji-kana dissociation is an essential part of the syndrome [14, 16, 17]. Imura also argued that the selective difficulty in kanji handling in Gogi aphasia is caused by its logographic nature, in which a single kanji character stands for multiple sounds and concepts simultaneously [16]. This complexity necessarily burdens a reader with the decision making to choose a correct pronunciation from possible candidates every time he has to read a sentence aloud.

      Responsible Lesions

      Imura speculated that responsible lesions for Gogi aphasia are rather diffuse, involving the second and third temporal gyri and adjacent parietal lobe on the left side [16].

      One of his cases (the above quoted case E) had been slowly deteriorating, leading Imura to presume a possibility of presenile dementia for its etiology [6]. The autopsy finding described by Pick of the case with “surdite verbale representative” (case F) which had also been slowly progressive showed the presence of diffuse cerebral atrophy, mainly affecting the left temporal lobe [15].